ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.9208A>G (p.Met3070Val)

dbSNP: rs1386338109
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001897731 SCV002148785 uncertain significance Cohen syndrome 2021-08-27 criteria provided, single submitter clinical testing

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